RT Journal Article SR Electronic T1 OP-8 A feasibility randomized controlled trial comparing opioid dose escalation vs. methadone addition for refractory cancer pain JF BMJ Supportive & Palliative Care JO BMJ Support Palliat Care FD British Medical Journal Publishing Group SP A6 OP A6 DO 10.1136/spcare-2024-ANZSPM.8 VO 14 IS Suppl 3 A1 Ikegami, Takako A1 Matsuoka, Hiromichi A1 Terada, Kosuke A1 Oyamada, Shunsuke A1 Ariyoshi, Keisuke A1 Matsubara, Naho A1 Ishikawa, Ayaka A1 Nishimura, Rumi A1 Kawasaki, Naruaki A1 Arakawa, Sayaka A1 Ishiki, Hiroto A1 Maeda, Makoto A1 Hashimoto, Hironobu A1 Miura, Tomofumi A1 Ishiguro, Hiroshi A1 Matsumoto, Yoshihisa A1 Satomi, Eriko YR 2024 UL http://spcare.bmj.com/content/14/Suppl_3/A6.1.abstract AB Background Cancer pain affects 38–85% of cancer patients, with higher incidence in advanced stages.1 Poorly controlled cancer pain, often with neuropathic elements, presents a significant unmet medical need. Despite various opioid formulations, 47% of physicians report difficulties in managing opioid-refractory pain.2 Methadone has shown superior efficacy to other opioids, such as morphine, especially for neuropathic pain poorly controlled by other opioids.3 Currently, opioid escalation is the standard, but is often inadequate, and although the methadone add-on (AO) method has been reported to be safe and effective for refractory cancer pain, no randomized controlled trials (RCTs) have been conducted.Aims This study aims to explore the feasibility of conducting a double-blind RCT to assess the efficacy and safety of the methadone AO method for opioid escalation in patients with cancer pain.Methods This study is a single-facility, double-blind, parallel-arm RCT. A total of 22 patients will be enrolled between July 2024 and September 2025. Eligible participants are adults with unresectable advanced cancer experiencing refractory cancer pain on an appropriate dose of opioid analgesia (60–300 mg oral morphine equivalent daily dose, OMEDD) and a Karnofsky Performance Status (KPS) >50. Participants will be randomized (1:1) to the methadone AO arm or the standard treatment arm. Evaluations will be conducted at baseline (randomization), day 1, 8, and 15. In the methadone AO arm, patients will receive over-capsulated methadone 5 mg or 10 mg, and in the 5 mg group, placebo will be used to unify the twice-daily dosing of the study drug. In the standard treatment arm, patients will receive over-capsulated oxycodone 10 mg or 20 mg. The primary endpoint is the completion rate of the two-week study treatment, defined as 70% or more. Secondary endpoints include changes in BPI scores before and after the study treatment and adverse events.Discussion Several considerations influenced the study design. First, the methadone dosage required careful determination. Previous studies suggest equivalence ratios of OMEDD 30–90 = 4:1, 90–300 = 6:1, and over 300 = 8:1. For this study, we set the morphine-to-methadone ratio at 6:1, which is safer than the 3:1 and 5:1 reported in other studies but less conservative than NCCN recommended 10:1. Second, the primary endpoint was defined as achieving a study completion rate of at least 70%. Although no prospective clinical trials exist, a Canadian cohort study (N=146) reported a continuation rate of 78.1% at Day 15 with a mean methadone dose of 6 mg. This data and discussions within our study group, led us to set a 70% completion rate. Finally, we chose a 2-week study period based on previous research: Mercadante et al. (n=108) found stable methadone doses over 4 weeks, and Bruera et al. (n=103) reported over 20% pain relief by Day 8 with no dose change between Days 14 and 28. Thus, 2 weeks is sufficient for efficacy and safety assessment. Based on the results of our study, we plan to conduct a larger-scale RCT of the methadone to establish a treatment for refractory cancer pain.ReferencesPoulain P, Berleur MP, Lefki S, et al. Efficacy and safety of two methadone titration methods for the treatment of cancer-related pain: The EQUIMETH2 Trial (Methadone for Cancer-Related Pain). J Pain Symptom Manage. 2016 Nov;52(5):626–636.e1Mercadante S, Porzio G, Ferrera P, et al. Sustained-release oral morphine versus transdermal fentanyl and oral methadone in cancer pain management. Eur J Pain. 2008 Nov;12(8):1040–6.Bruera E, Palmer JL, Bosnjak S, et al. Methadone versus morphine as a first-line strong opioid for cancer pain: a randomized, double-blind study. J Clin Oncol. 2004 Jan 1;22(1):185–92.